Didelphys uterus
Synonyms: Bicervical bicornuate uterus
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare non-syndromic uterovaginal malformation characterized by two separate uterine cavities and cervices, due to failure of the Müllerian ducts to fuse. A longitudinal vaginal septum of variable thickness and elasticity is also present. Patients may be asymptomatic or experience dyspareunia or dysmenorrhea. There is increased frequency of endometriosis, as well as fertility and gestational issues with significantly reduced chances of seeing a pregnancy to term. The condition may be associated with renal agenesis.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Didelphys uterus | Bicervical bicornuate uterus |
| fr | Utérus didelphe | Utérus bicorne bicervical |
| de | Uterus Didelphys | Uterus bicornis, bizervikaler |
| es | Útero didelfo | Útero bicorne bicervical |
| it | Utero didelfo | Utero bicorne bicervicale |
| nl | Uterus didelphys | Bicervicale tweehoornige baarmoeder |
| pt | Útero didelfo | |
| pl | Macica podwójna | Macica dwurożna dwuszyjkowa |
| cs | Uterus duplex didelphys | = en |
| uk | Матка Didelphys | Біцервікальна дворога матка |
| zh | 双子宫 | 双宫颈双角子宫 |
| tr | Didelfis uterus | Bikervikal bicornuat uterus |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q51.1 | E | specific | validated |
| ICD-11 | LB44.3 | NTBT | index | validated |
| MONDO | 0015834 | E | validated | |
| MeSH | D000093642 | E | validated | |
| UMLS | C0266393 | E | validated | |
| MedDRA | 10012770 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:180134Bicornuate uterus
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare gynecological and obstetric diseases; rare transplant-related disorders
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180086
- This record as JSON: /data/d/180086.json